Hepatitis B, C, and D virus and human T-cell leukemia virus types 1 and 2 infections and correlates among men who have sex with men in Ouagadougou, Burkina Faso

A cross-sectional survey was conducted among MSM recruited using respondent driven sampling (RDS). RDS is a peer-recruitment sampling method designed to collect rigorous, representative data from hard-to-reach populations [29‐31]. In preparation for this first integrated biological and behavioral survey, formative pre-survey research was conducted using formal meetings with MSM, local organizations, and government officials to explore MSM’s willingness to recruit their peers, challenges in finding diverse segments of this hidden population, and preferences expressed by MSM for all study procedures. The results of these meetings suggested that RDS should be used for the survey.

The survey took place in Ouagadougou, the capital of Burkina Faso, a West African country with limited resources and high burden of viral hepatitis B and C.

MSM were eligible to participate if they meet the following criteria: (i) at least 18 years old, (ii) assigned male gender at birth, (iii) reported anal sex with a man at least once in the past 12 months, (iv) able to provide informed consent in French, Mòoré, or Dioula, (v) had a valid coupon, (vi) lived in Ouagadougou for at least the past three months, and (vii) agreed to complete a behavioral questionnaire and human immunodeficiency virus (HIV) testing.

Recruitment chains were initiated by MSM seeds. Six MSM seeds were purposely selected. Seeds were chosen who met the study eligibility criteria, represented diverse demographics (age, education, marital status, language, and HIV status), and who were willing to promote the study.

After giving informed consent, seeds were required to complete a questionnaire and have their blood drawn. These seeds were each provided with three coded coupons which were valid for four weeks to recruit MSM peers from their social network. Individuals who were recruited by seeds and enrolled in the study were then provided with three coded coupons for further recruitment of peers. This process continued until the target sample size was reached.

Participants received male condoms, condom-compatible lubricants, HIV education materials, and information regarding existing services. They also received 2000 XOF (~$4 United States dollars [USD]) for their time and transportation costs for each study visit. Per successfully eligible peer recruited to be part of the study (for up to three peers), recruiter had received 1500 XOF (~$3 USD). To avoid individuals participating multiple times, a single study office was used in addition to the use of a unique identification code. Study staff included a site manager, a coupon manager, two data collectors, an HIV and STI test counselor, and a lab technician. All staff were trained in the study procedures to avoid duplicate enrollments.

Sample size was previously estimated from an HIV behavior and seroprevalence study. The recruitment framework entailed 350 MSM. This size calculation was based on the assumption that populations who always use condoms have a 75% lower HIV prevalence than populations who do not, and the effectiveness of condoms is roughly 80%, with 73% used as a conservative estimate [32]. Overall, HIV prevalence was estimated at 15% with 19% prevalence among those who did not consistently use condoms. A design effect of 1.5 associated with RDS, significance level of 0.05, and a power of 80% was used.

Data were collected from January to April 2013 in Ouagadougou. Following informed consent, MSM participants completed interviewer-administered face-to-face questionnaires in a private room. Information included socio-demographic characteristics of participants, partnerships and sexual behaviors (with men and women), condom use, knowledge, attitudes and practices related to STI, and injection drug use.

A trained nurse and lab technician respectively conducted HIV/STI counseling, venous blood specimen collection and HIV and syphilis testing in the study office. Serum samples were stored at − 20 °C et transported to the laboratory for hepatitis B, C, D and HTLV testing using DiaPro Enzyme Linked Immunoassay (ELISA) methods (https://​www.​diapro.​it,). All tests were performed according to the manufacturer’s instructions.

The ELISA test kit HBsAg One version ULTRA (ULTRA-Dia.Pro, Diagnostic BioProbes Srl, Italy), able to detect HBV “s” mutant was used for hepatitis B surface antigen detection. This test uses a mix of mouse monoclonal antibodies specific to determinants “a”, “d”, and “y” of HBsAg fixed to the surface of microwells. For test procedure, 150 μl of serum were added to the microwell together with 100 μl of a second mix of mouse monocolonal antibodies, conjugated with Horseradish Peroxidase (HRP) and directed against a different epitope of the determinant “a” and against “preS”. The specific immonocomplex, formed in the presence of HBsAg in the sample, is captured by the solid phase. At the end of of the one-step incubation for 120 min at 37 °C, microwells were washed to remove unbound serum proteins and HRP conjugate. Then 200 μl of chromogen/substrate (tetra-methyl-benzidine and hydrogen peroxidase, TMB/H2O2 mix) were added and incubate for 30 min at room temperature. In the presence of captured HBsAg immunocomplex, the colorless substrate is hydrolyzed by the bound HRP conjugate to a colored end-product. After blocking the enzymatic reaction by adding 100 μl of sulfuric acid, its optical density was measured with the ELISA reader (Reader 270, Microelisa system, Biomerieux, France) using 450 nm filter for raiding and a 620 nm filter for background subtraction. by the ELISA reader. The color intensity is proportional to the amount of HBsAg present in the sample.

HBsAg reactive samples were subsequently tested for detection of anti-HDV antibodies using HDV Ab Dia.Pro, Diagnostic BioProbes Srl, Italy test kit, a competitive ELISA methods. The antibodies present in the serum compete with a virus-specific polyclonal IgG, labelled with peroxidase (HRP), for a fixed amount of rec-HDV coated on the microplate. The test was carried out with two steps incubation competitive system. First the 100 ul of sample were added to the plate and specific anti-HDV antibodies bind to the adsorbed antigen and incubated for 60 min at 37 °C. After washing (4–5 cycles), 100 μl of an enzyme conjugate antibody to HDV were added and binds to the free portion of antigen coated, following by second incubation for 60 min at 37 °C. After washing, 100 μl of chromogen/substrate mixture (TMB/H2O2 mix) was dispensed and incubated for 20 min at lab temperature (25°). The concentration of the bound enzyme on the solid phase becomes inversely proportional to the amount of anti-HDV antibodies in the sample and its activity was detected by the added chromogen/substrate. After blocking the enzymatic reaction by addition of 100 μl of sulfuric acid, the optical density was measured with the ELISA reader using a 450 nm filter for raiding and a 620 nm filter for background subtraction. The concentration of of HDV-specific antibodies in the sample is determined by means of a cut-off value that allowed for the semi-quantitative detection of anti-HDV antibodies.

For anti-HCV antibodies, the fourth generation ELISA HCV Ab-Dia.Pro test (Diagnostics BioProbes Srl, Italy) was used. This test kit uses microplates coated with HCV-specific antigens derived from “core” and “n” regions encoding for conservative and immunodominant antigenic determinants (core peptide, recombinant NS3, NS4 and NS5 peptides). The solid phase was first treated with the diluted sample (200 μl diluent + 10 μl sample) and incubated à 37 °C, 45 min. HCV antibodies were captured, if present, by the antigens. After washing out all the other components of the sample, in the second incubation (45 min, 37 °C) bound HCV antibodies, immunoglobin G and M as well, were detected by addition of 100ul of polyclonal specific and hIgG&M antibodies, labelled with peroxidase (HRP). The enzyme captured with on the solid phase, acting on the chromogen/substrate mixture (100ul of TMB/H2O2), generates an optical signal that was proportional to the amount of anti HCV antibodies present in the sample. After incubation at lab temperature (25 °C) for 15 min, 100 μl of sulfuric acid were added into each well to stop the enzymatic reaction. The optical density was measured with the ELISA reader using 450 nm filter for raiding and a 620 nm filter for background subtraction. A cut-off value let densities was interpreted into HCV antibodies negative and positive results.

Anti-HTLV 1&2 antibodies were tested using the ELISA HTLV 1&2 Ab-Dia.Pro ULTRA version (Diagnostic BioProbes Srl, Italy). This test uses microplates coated with HTLV1&2 specific synthetic immunodominant antigens derived from gp46–1, gp46-II and gp21-I. The solid phase was first treated with the sample (100 μl) and anti-HTLV 1&2 antibodies are captured during incubation (for 45 min at 37 °C) by the antigens coated on the microplate. After washing out all the other components of the sample, in the second incubation for 45 min at 37 °C, bound anti-HTLV 1&2 total antibodies was detected by the addition 100 μl of specific synthetic antigens derived from gp46–1, gp46-II and gp21, labelled with peroxidase (HRP). The enzyme captured on the solid phase, acting on the chromogen/substrate mixture, generates an optical signal that is proportional to the amount of anti HTLV 1&2 antibodies present in the sample. After blocking the enzymatic reaction, its optical density was measured by the ELISA reader (OD 450 nm).

For each testing, manufacturer negative and positive controls, and calibrator were used. The results were calculated by the means of a cut-off value (Co) determined on the mean optic density (OD) 450 nm value of the negative control as recommended in the kit manufacturer procedure. The test results were interpreted as positive when a ratio of the samples optic density at 450 nm (S) and the cut-of-value (Co) was superior to 1.1. Assay procedure was repeated for sample with equivocal result (S/Co = 0.9 to 1.1). All repeated testing provided negative or positive result and have been considered.

Data were entered using EpiData 3.1 (The EpiData Association, Odense, Denmark) and exported into Stata 14 (StataCorp, College Station, TX) for analysis.

Descriptive statistics were used to describe participants’ characteristics, HBV, HCV, HDV and HTLV 1&2 seroprevalence, and sexual behaviors. All proportions were adjusted to account for the RDS method. This adjustment takes into consideration the probability of each participant to be included in the study. This probability was measured through weighting based on the size of each participant’s network. Network size was determined using the survey question: “How many different people do you know personally who are MSM? i.e., you know them and they know you, you have seen them in the last 2 years, and you could contact them if you needed to?” The mean network size of study participants was 17 (minimum = 1 and maximum = 600). Population estimates and 95% CI adjusted for the RDS design were produced using the RDS Analysis Tool (RDSAT) version 6.0.1 (RDS, Inc., Ithaca, NY).

The study received ethical approval from the Ethics Committee for Health Research (CERS) of Burkina Faso. The study was implemented in a secure setting, and questionnaires were conducted in a private office. Collection of blood samples was performed by a trained staff member. Research ethic and sensitivity training were provided to all study staff before study implementation. Confidentiality was maintained by using a unique study identifier rather than real names on questionnaires and all study materials, protecting all electronic data with passwords, and storing hard copies of data in locked cabinets. Participant unique and anonymized codes were used to link study questionnaires with blood samples. All participants who tested positive for HIV were referred to a healthcare center.

Participants’ socio-demographic characteristics are presented in Table 1. The mean age was 22.9 ± 4.0 years. In terms of sexual orientation, 71.9% (95% CI: 66.7–76.5) of MSM reported being gay/homosexual. Less than half of the study participants were bisexual (44.1%; 95% CI: 38.9–48.9). A minority (2.1, 95% CI: 0.0–4.4) were transgender. The majority of study participants were single (94.6, 95% CI: 91.6–96.5). Most of them were born in Burkina Faso. Over 70% (71.8, 95% CI: 66.8–76.4) of the participants recruited were students or pupils, while employees represented 21.6% (95% CI: 17.3–26.3).

Tables 2 and 3 present the seroprevalence and factors associated with HBV, HCV and HTLV 1&2 in the bivariate and multivariate analyses.

The prevalence of HBV among MSM was estimated at 20.4% (95% CI: 16.4–25.1). Bivariate analyses showed that the factors associated with HBV infection were reporting multiple sexual partnerships with at least two male partners and a female sexual partner (p = 0.010), experiencing condom tearing during anal sex (p = 0.035), not using a condom at last anal sex with a main male sexual partner (p = 0.029), and being divorced, widowed, married or cohabiting with a woman (p = 0.023). Multivariate analysis showed that only not using a condom at last anal sex with a main male sexual partner (p = 0.033) and experiencing condom tearing during anal sex (p = 0.012) were independently associated with HBV infection (Table 3).

The prevalence of HCV among MSM is estimated at 11.0% (95% CI: 8.0–14.8). Although patterns of disparity were observed according to some characteristics of MSM, bivariate and multivariate analyses with study variables did not reveal any factors associated with HCV infection among MSM (Table 3).

Anti-HDV antibody testing was performed on HBV-positive samples. No participants tested positive for anti-HDV antibodies, meaning that the seroprevalence was 0.0%.

The results show that the seroprevalence of the HTLV virus in the MSM surveyed is estimated at 4.0% (95% CI: 2.3–6.8). In the bivariate analysis, the factors associated with HTLV 1&2 infection were a history of STI symptoms (genital lesions) during the last 12 months (p = 0.001), not using a condom at last anal sex with a main male sexual partner (p = 0.017), and not using a condom at last anal sex with a casual male sexual partner (p = 0.018). Only the history of genital lesions (penis or anus) during the last 12 months and injection drug use were independently associated with the seroprevalence of anti-HTLV 1&2 antibodies in the multivariate analysis (Table 3).

The prevalence of HBV (20.4%) in our sample of MSM is higher than those reported among other populations in Burkina Faso. In a recent systematic review in Burkina Faso covering the period from 1996 to 2017, the authors estimated the prevalence of HBV at 9.41% among the general population, 11.11% among pregnant women, 11.73% among blood donors and 12.6% among people living with HIV [33]. Our results suggest that MSM are a vulnerable group for HBV infection. Modes of transmission other than vertical transmission may explain the high prevalence of HBV among MSM [7, 11, 12]. In this study, the factors associated with HBV infection in the bivariate analysis were for the most part, factors related to sexual behavior, including multiple sexual partnerships with male and female partners, in addition to age ≥ 30 years and marital status with a woman. Older age had already been identified in some studies as associated with HBV infection [6, 7, 34], and could be explained by the accumulation of risk of exposure over time and vaccination against HBV coverage, which is increasing among younger individuals. Vaccination against HBV was only introduced in Burkina Faso in 2006 for infants [33].

The majority of MSM in our study identified themselves as gay, but over 44% reported being bisexual and have sex with men and women, and some are in a conjugal relationship with women. Bisexual MSM could have a higher risk of transmitting and acquiring STI [35], which could explain the higher prevalence of HBV infection among married MSM.

Multivariate analysis in our study showed that only condom use at last anal sex with a main male sexual partner (p = 0.033) and condom tearing during anal sex (p = 0.012) were independently associated with HBV infection, suggesting transmission of the virus through high-risk sex.

In our study, no HBsAg-bearing MSM was infected with HDV. A prior study found a 0.1% (95% CI: 0.06–0.23) HDV prevalence among men in general population of Burkina Faso [36]. The very low prevalence in our study could be explained by the small size of the sample. However, although the number of positive HBsAg samples analyzed in our study is low, zero seroprevalence of anti-HDV antibodies has also previously been reported by studies in Sub-Saharan Africa. An analysis of 49 pregnant women with HBsAg in Burkina Faso revealed no evidence of anti-HDV antibodies [37]. Similarly, in Mozambique, Cunha et al., in their study of 146 blood donors infected with HBV, found no positive cases of anti-HDV antibodies [38].

West Africa is considered an area with a high prevalence of HCV [39, 40]. We found in our study a prevalence of 11% in MSM. This prevalence is three times higher than that reported in Burkina Faso, and in West Africa in general. An analysis of the blood samples collected during the 2010 Demographic and Health Survey in the Burkinabe population estimated the HCV prevalence at 3.6% [41]. Systematic reviews have also estimated the pooled prevalence of HCV in the West African population between 3 and 5% [39, 42]. HCV transmission is mainly through blood, especially through transfusion with contaminated blood or nosocomial transmission with contaminated material [18]. Among MSM, there is often an increased risk of infection from injection drug use and HIV infection [8, 9, 43, 44]. In a recent systematic review, the authors found that the prevalence of anti-HCV antibodies was estimated at 40 and 6.7%, respectively, among HIV-positive MSM who were injection drug users and non-drug users [45]. Furthermore, traumatic anal sex may be involved in HCV transmission among MSM.

HTLV 1&2 viruses are probably among the most neglected bloodborne viruses among MSM in Africa, and data are very scarce. This first study of MSM in Burkina Faso shows that the overall seroprevalence of anti-HTLV 1&2 antibodies was 4%. This seroprevalence is higher than those reported among pregnant women in West Africa, especially in Burkina Faso in 2006 (1.02%), in Côte d’Ivoire in 1989 (1.9%), and in Ghana in 2006. (2.1%) [23]. More recently in Nigeria, Yuguda et al. reported a seroprevalence of 3.2% among blood donors in Nigeria, with all positive cases being male [46]. The high prevalence of anti-HTLV 1&2 antibodies in MSM in our study may be explained by risk behaviors [26, 47]. The factors independently associated with the presence of anti-HTLV 1&2 antibodies in our study were a history of genital lesions (penis or anus) during the last 12 months and injection drug use. Other authors have found that HTLV infection in MSM is associated with the presence of STI including syphilis or genital lesions [14, 48, 49], or injection drug use. In a study in Argentina among people who inject drugs, MSM, sex workers, and tuberculosis patients, the authors found an overall prevalence of anti-HTLV 1&2 antibodies of 2.4%, and the highest prevalence (19.1%) was among people who inject drugs [27].

Our study has a number of limitations. Participants may have underreported sensitive behaviors, including injection drug use, which is punishable by law in Burkina Faso. The study was cross-sectional, therefore it is unknown whether the identified risk factors preceded the associated infections. Also, in this seroprevalence study, the testing was based on serological methods using fourth generation ELISA. Even these methods have very high specificity and sensitivity, a positive HBsAg or HCV and HTLV antibody test does not confirm the stage of infection during the study. Finally, there are specific limitations to the RDS method. The RDS financial incentive, while modest, may encourage more low-income MSM to participate in the study and lead to selection bias. Despite these limitations, RDS was identified during the preparatory phase of data collection as the best approach to recruiting MSM in this context. In addition, our study provides the first seroprevalence data for hepatitis B, C, and D and HTLV viruses among MSM in Burkina Faso. These data fill a gap and will help map the epidemiology of these infections among high-risk populations in Africa.